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Trifluoroacetic acid → (2-Chloro-phenyl)-(3-hydroxy-pyridin-2-yl)-methanone

HRID 2251988
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HRID 2251988 반응식
FC(F)(F)C(O)=O.[Cl:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]([C:17]1[C:22]([O:23]COCC[Si](C)(C)C)=[CH:21][CH:20]=[CH:19][N:18]=1)=[O:16]>C(Cl)Cl>[Cl:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]([C:17]1[C:22]([OH:23])=[CH:21][CH:20]=[CH:19][N:18]=1)=[O:16]
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 69153886(2-Chloro-phenyl)-[3-(2-trimethylsilanyl-ethoxymethoxy)-pyridin-2-yl]-methanone

생성물 1

HCID 69154628(2-Chloro-phenyl)-(3-hydroxy-pyridin-2-yl)-methanone수율 82%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Add trifluoroacetic acid (5 mL) to a solution of (2-chloro-phenyl)-[3-(2-trimethylsilanyl-ethoxymethoxy)-pyridin-2-yl]-methanone (195 mg, 0.54 mmol) in CH2Cl2 (3 mL), stir for 30 minutes. Concentrate; dissolve in 20% i-PrOH/CHCl3, wash with saturated NaHCO3 solution (×2). Dry the combined organic layers over MgSO4 and concentrate. Purify the residue by flash chromatography on silica gel eluting with 0-30% Et2O/hexanes to afford the title compound (102 mg, 82%) as white solid. MS(IS) 233.9 (M+1). TLC: Rf=0.20 (25% Et2O/hexanes).

후처리

  1. concentrationConcentrate
  2. dissolutiondissolve in 20% i-PrOH/CHCl3
  3. washwash with saturated NaHCO3 solution (×2)
  4. dry with materialDry the combined organic layers over MgSO4
  5. concentrationconcentrate
  6. customPurify the residue by flash chromatography on silica gel eluting with 0-30% Et2O/hexanes

출처 및 근거

ORD 기록
ord-be369d308a2d4d968dd8ea0bd68f9a05
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07320994B2

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